The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
124535082 12453508 2 F 2012 20151103 20160609 20160720 PER US-DSJP-DSU-2015-125985 DAIICHI 0.00 F Y 76.19000 KG 20160718 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
124535082 12453508 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 UNK U 21532 FILM-COATED TABLET
124535082 12453508 2 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 40-25 MG ONCE DAILY U 21532 FILM-COATED TABLET
124535082 12453508 3 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 20-12.5 MG ONCE DAILY U 21532 FILM-COATED TABLET
124535082 12453508 4 SS BENICAR OLMESARTAN MEDOXOMIL 1 Oral 40 MG, QD 0 40 MG TABLET QD
124535082 12453508 5 C ASPIRIN /00002701/ ASPIRIN 1 325 MG, QD 0 325 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124535082 12453508 1 Hypertension
124535082 12453508 4 Product used for unknown indication
124535082 12453508 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124535082 12453508 Adenoma benign
124535082 12453508 Anaemia
124535082 12453508 Dizziness
124535082 12453508 Dyspepsia
124535082 12453508 Early satiety
124535082 12453508 Gastritis
124535082 12453508 Malabsorption
124535082 12453508 Regurgitation

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
124535082 12453508 1 2010 0
124535082 12453508 2 201302 20150514 0